US2238486A - Azo compounds and material colored therewith - Google Patents

Azo compounds and material colored therewith Download PDF

Info

Publication number
US2238486A
US2238486A US304138A US30413839A US2238486A US 2238486 A US2238486 A US 2238486A US 304138 A US304138 A US 304138A US 30413839 A US30413839 A US 30413839A US 2238486 A US2238486 A US 2238486A
Authority
US
United States
Prior art keywords
group
azo
azo compounds
member selected
cellulose
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US304138A
Inventor
Joseph B Dickey
Jr John R Byers
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US304138A priority Critical patent/US2238486A/en
Application granted granted Critical
Publication of US2238486A publication Critical patent/US2238486A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling

Definitions

  • the presentinvention relates to ace dyestuffs and to organic derivatives of cellulose colored therewith. More particularly it relates to nonsulfonated nuclear azo compound-sof the benzene and naphthalene series containing in their mole cule at least oneaminogroup in para position to an azo bond, and at least onegroup of thegeneral formula: V t I --!RO- CO- N-I-Iz whreinr-R represents an aliphatic group joined .dir'ectlyto or :through an oxygen linkage, .a;nitro gen linkage, a nitrogen-sulphur linkage, .ora nitrogen-carbon linkage to one of the nuclei of the molecule.
  • n is an integer.
  • Furthermorathenuclei of the azo compounds above described may be substituted by one or more other monovalentsubstituents selected from the group of atoms such as chlorine, bromine, fluorine, and radicals such as a hydroxyl group, a methyl group, an ethyl group, a butyl group, a methoxy group, an ethoxy group, an acetyl group, an acetamino group, a carbamide group, and the like;
  • the diazo component may be p-aminoazobenznebr a substituted derivative of p-aminoazobenzene having *l'iOg'SlllDhOIliC acid group and whose diazo salt is capable of being coupled.
  • the necessary intermediates containing the carbamic acid ester grouping wherein R. has the meaning previously defined may be prepared by a number of methods including the'process of condensing an arylamine having a hydroxyalkyl side chain group with urea or carbamyl chloride.
  • ethyl-c-hydroxyethylaniline may be condensed with carbamyl chloride, and the corresponding carbamic acid ester thereby produced may be coupled with the desired aryl diazo compound in the usual manner, or, the azo compound may first be prepared followed by condensation with urea or with carbamyl chloride.
  • Example '1 g 1 mole of p-aminoacetop-henone is diazotized with sodium nitrite and the solution added toa :mixture of ice and water containing hydrochloric acid and approximately 1 mole of the carbamic acid ester of ethyl-e-hydroxyethylaniline. After standing for a relatively short time, the reaction 7 acetate iscolored orange shades from an aqueous suspension of the dye.
  • the azo compound obtained has the formula:
  • Example 2 1 mole of p-nitroaniline is diazotizedand coupied with 1 mole of the carbamic acid ester ethyl ample 1.
  • the azocompound obtained has the formula:
  • Example 3 1 mole of p-nitro-o-chloroaniline is diazotized and coupled with 1 mole of the carbamic acid ester of di-fl-hydroxy-ethyl-m-toluidine following the procedure of Example 1. Cellulose acetate is colored rubine shades from an aqueous suspension of the dye.
  • the azo compound obtained has the formula:
  • the azo compound obtained has the formula:
  • Example 5 In a similar manner there may be prepared an aryl azo carbamate which has the formula:
  • the invention is illustrated further by the fol- No lowing additional azo compounds which may be ⁇ czmo CH3 30 prepared in a manner similar to that described in Example 1. These compounds color cellulose CH1 0 acetate the shades of color designated.
  • the dyes are ordinarily appliedto' the V materials from their aqueous solutionsor suspensions. If the particular dye is insoluble or only H2N N- N-N slightly soluble in Water, it is first groundtoa 40 ⁇ CflLOCONm paste with a dispersing agent such. as a soap, a 01 u at d LO a higher fatty acidgl'y y are; ground with 9 parts'of a dispersing agent fate, and the resulting paste then.
  • a dispersing agent such. as a soap, a 01 u at d LO a higher fatty acidgl'y y are; ground with 9 parts'of a dispersing agent fate, and the resulting paste then.
  • the dispersion is th n e d to a sulting paste dispersed in 3000 parts of water. perature of about -55" C., the material im- 45
  • the dispersion thus prepared is heated to atemme ed t e d the tempe atu g l y perature approximating 40-50 C., and 100 parts increased to aboutSO-85 C., at which point the of cellulose acetate fabric is immersed therein. material is worked for several hours.
  • Salt may The temperature is then gradually raised to be added to facilitate exhaustion of the dye bath YO-80 C., and the fabric worked at this temduring the dyeing operation. When the material perature until the desired shade or condition of. has attained the desired shade or condition of yellow color is acquired. It is then removed color, it is removed from the bath, washed with from the bath, rinsed with water, and diazotized soap, rinsed and dried.
  • the dyeing operasisting of 6 parts of sodium nitrite, 15 parts of tion may be performed in an aqueous solution of hydrochloric acid of 20 B., and 3000 parts of the dye containing salt without the necessity of water.
  • the employing any k of dispgrsing -or solubilizing fabric is Well rinsed with water and developed toagent a deep black.
  • the dye compounds of the invention which e st rting with e hi bath n r duhave a free amino group as a nuclear substituent any Increasing to a fi ng temperature 05 thereof may be applied to the material to be 60 m a i frl i 6 part of colored in the manner above described, followed i' 'g'gzgg pans 9 sodmm' thereafter by diazotization and coupling in situ s fi g g gy i g if n t t v with couplers such as c-hydmxy-S-naphthoic r S m ed m t due black Shades of color
  • couplers such as c-hydmxy-S-naphthoic r S m ed m t due black Shades of color
  • R1-N NR2 wherein R1 represents an aryl nucleus of the benzene series, R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
  • R represents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -R-OCONH2.
  • R1 and R2 each represents an aryl nucleus of the benzene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
  • R represents an aliphatic group joined to the molecule through a member selected from the group consisting of 1/ O J O 1 n n o-, N, fiN-, ON
  • R1 represents an aryl nucleus of the benzene series
  • R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the formula:
  • R represents an aliphatic group joined to the molecule through an oxygen atom.
  • R1 and R2 each represents an aryl nucleus of the benzene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the formula:
  • R represents an aliphatic group
  • R1 and R2 each represents a benzene nucleus
  • R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group R-OCONH2.
  • each :1: represents a member selected from the group consisting of hydrogen, a halogen, a hydroxyl group, an alkyl group, and a nitro group
  • R represents an aliphatic group
  • R2 represents a benzene nucleus
  • R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -RO-CONH2.
  • R1 represents an aryl nucleus of the benzene series
  • R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
  • R represents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group R- OCONH2.
  • R1 represents an aryl nucleus of the benzene series
  • R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
  • R rep-resents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -R-OCO-NH2.
  • R represents an aliphatic group
  • R1 and R2 each represents a benzene nucleus
  • R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -RO-CONH2.
  • R represents an aliphatic group
  • R1 and R2 each represents a benzene nucleus
  • R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group --RO-CONH2.
  • m represents a member selected from the group consisting of hydrogen, a halogen, a hydroxyl group, an alkyl group, and a mtro group
  • R represents an aliphatic group
  • R2 represents a benzene nucleus
  • R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a. hydroxyalkyl group, and the group R-O--CONH2.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

Patented Apr. 15, 1941 AZO COMPOUNDS AND MATERIAL ooconsn THEREWITH Joseph B. Dickey and John R. Byers, Jr., Rochester, (N. Y., assignors to Eastman Kodak -Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application Novemberl3, 1939,
'Serial No. 304,138
, 12 Claims.
The presentinvention relates to ace dyestuffs and to organic derivatives of cellulose colored therewith. More particularly it relates to nonsulfonated nuclear azo compound-sof the benzene and naphthalene series containing in their mole cule at least oneaminogroup in para position to an azo bond, and at least onegroup of thegeneral formula: V t I --!RO- CO- N-I-Iz whreinr-R represents an aliphatic group joined .dir'ectlyto or :through an oxygen linkage, .a;nitro gen linkage, a nitrogen-sulphur linkage, .ora nitrogen-carbon linkage to one of the nuclei of the molecule. member selected from the group consisting of a methylene group, an ethylene group, a propylene group, and groups represented by the structural formulae CHzCH-,CHg-CHCl1a,CilIiOH OHz, I on on -onz onon),-oniwherein n is an integer. Furthermorathenuclei of the azo compounds above described may be substituted by one or more other monovalentsubstituents selected from the group of atoms such as chlorine, bromine, fluorine, and radicals such as a hydroxyl group, a methyl group, an ethyl group, a butyl group, a methoxy group, an ethoxy group, an acetyl group, an acetamino group, a carbamide group, and the like;
The expressions oxygen linkage? nitrogen linkage, nitrogen-sulphurlinkage, and nitrogen-carbon linkage? are intended tothroughout thefspeoification and claims unless otherwise specified that R in the above formula is joined to a nucleus of the, am compound through an intervening atom or group of atoms represented structurally by v N I wherein 1: stands for hydrogeman alkyl group,'a hydroxyalkyl group,'and the group 1 While our invention is primarily concerned with the monoazo compoundspoly-azo compounds are likewise included within the scope ofithein-F' More specifically R represents a mean vention. For example,the diazo component may be p-aminoazobenznebr a substituted derivative of p-aminoazobenzene having *l'iOg'SlllDhOIliC acid group and whose diazo salt is capable of being coupled.
We have found that the azo compounds-described in the preceding are excellent dyes which produce on textile materials colors of excellent fastness to light and high resistance to washing, and burnt gas fumes. ,It is an object of our invention, therefore, to prepare this class of azo dyestufisand to color organic derivatives of cellulose especially cellulose acetate, therewith.
The necessary intermediates containing the carbamic acid ester grouping wherein R. has the meaning previously defined, may be prepared by a number of methods including the'process of condensing an arylamine having a hydroxyalkyl side chain group with urea or carbamyl chloride. For example, ethyl-c-hydroxyethylaniline may be condensed with carbamyl chloride, and the corresponding carbamic acid ester thereby produced may be coupled with the desired aryl diazo compound in the usual manner, or, the azo compound may first be prepared followed by condensation with urea or with carbamyl chloride. I
The following examples illustrate the prepara-' tion of some of theazo compounds of our invention.
, Example '1 g 1 mole of p-aminoacetop-henone is diazotized with sodium nitrite and the solution added toa :mixture of ice and water containing hydrochloric acid and approximately 1 mole of the carbamic acid ester of ethyl-e-hydroxyethylaniline. After standing for a relatively short time, the reaction 7 acetate iscolored orange shades from an aqueous suspension of the dye.
The azo compound obtained has the formula:
Example 2 1 mole of p-nitroaniline is diazotizedand coupied with 1 mole of the carbamic acid ester ethyl ample 1.
The azocompound obtained has the formula:
omcuoncmooomu Example 3 1 mole of p-nitro-o-chloroaniline is diazotized and coupled with 1 mole of the carbamic acid ester of di-fl-hydroxy-ethyl-m-toluidine following the procedure of Example 1. Cellulose acetate is colored rubine shades from an aqueous suspension of the dye.
The azo compound obtained has the formula:
CzHrOH l I CzHiO C ONH: Cl CH3 Example 4 1 mole of 4-nitro-2-methylaniline is diazotized and coupled with 1 mole of 2-e-methoxyethylamino-benzyl carbamate following the procedure described in Example 1. Cellulose acetate is colored orange shades from an aqueoussuspension of the dye.
The azo compound obtained has the formula:
Example 5 In a similar manner there may be prepared an aryl azo carbamate which has the formula:
I (321140 C ONE) and colors cellulose acetate red shades from an aqueous suspension of the dye.
g The invention is illustrated further by the fol- No lowing additional azo compounds which may be \czmo CH3 30 prepared in a manner similar to that described in Example 1. These compounds color cellulose CH1 0 acetate the shades of color designated.
Shade on Diazo component Coupling component cellulose acetate H p-Nltro-o-fluoroamlme N\ I Red.
CHaOHGHa CH3 I O C ONH:
C2H4O 03H) C ONE: p-Nitro-o-bromoaniline H0 Blue.
CH p-Nitro-o-chloroaniline N\ Rubine.
O C2H4O C ONHQ CHzCHCHzOH N O O NHz p-Nitro-o-hydroxyanillne CH". Pink.
0 C1H4O C O NH:
/H p-Nitro-o-hydroxyethylsulfone aniline QN\ Violet.
CzH4GHC-H2O 0 ONE; C Ha I O OH; /C 21140 C ONH: 2,4-dinitroaniline -N\ Blue.
621340 0 0 N H1 NBC ONH:
. H 2,4-d1mtro-6-hydroxyamlme -N\ D0.
OHzOHOHOHzO C ONHa Shadeon Diazo component Coupling component cellulose acetate 00111 i /C2H5 2,4-dinitro-G-fluoroaniliue C N\ Purple.
CaH4OCzH4QCONE-Ii CH3 7 0611s /C2H5 2,i-dinitro-G-chloroaniline N Blue. CHaCHOHCHzOCONH: Nnoooni I H Do N\ Violet.
I CafluOCONH;
cimoc ONE,
Do Blue.
(Ilia- CH1 Griz-H CH1 p-Aminoazobenzene 0 Rubme.
1 cnxononnoncnlocomh 3 000N111 In the application of the azo compounds of the Example 6- invention to the coloration of organic derivatives 2 parts of of cellulose, the dyes are ordinarily appliedto' the V materials from their aqueous solutionsor suspensions. If the particular dye is insoluble or only H2N N- N-N slightly soluble in Water, it is first groundtoa 40 \CflLOCONm paste with a dispersing agent such. as a soap, a 01 u at d LO a higher fatty acidgl'y y are; ground with 9 parts'of a dispersing agent fate, and the resulting paste then. dispersed in h as soap or oleyl glyceryl sulfate and th water. The dispersion is th n e d to a sulting paste dispersed in 3000 parts of water. perature of about -55" C., the material im- 45 The dispersion thus preparedis heated to atemme ed t e d the tempe atu g l y perature approximating 40-50 C., and 100 parts increased to aboutSO-85 C., at which point the of cellulose acetate fabric is immersed therein. material is worked for several hours. Salt may The temperature is then gradually raised to be added to facilitate exhaustion of the dye bath YO-80 C., and the fabric worked at this temduring the dyeing operation. When the material perature until the desired shade or condition of. has attained the desired shade or condition of yellow color is acquired. It is then removed color, it is removed from the bath, washed with from the bath, rinsed with water, and diazotized soap, rinsed and dried. If on the other hand the during 20 to 30 minutes in a fresh cold bath conparticular dye is water-soluble, the dyeing operasisting of 6 parts of sodium nitrite, 15 parts of tion may be performed in an aqueous solution of hydrochloric acid of 20 B., and 3000 parts of the dye containing salt without the necessity of water. After the diazotization is complete, the employing any k of dispgrsing -or solubilizing fabric is Well rinsed with water and developed toagent a deep black. color over a period of about 30 min- The dye compounds of the invention which e st rting with e hi bath n r duhave a free amino group as a nuclear substituent any Increasing to a fi ng temperature 05 thereof may be applied to the material to be 60 m a i frl i 6 part of colored in the manner above described, followed i' 'g'gzgg pans 9 sodmm' thereafter by diazotization and coupling in situ s fi g g gy i g if n t t v with couplers such as c-hydmxy-S-naphthoic r S m ed m t due black Shades of color The to connection with the dyeing of cellulose acetate 0 t b in? silk, it will be understood that the same processes 10W1ngexamp e 1 m f a are not limited exclusively to cellulose acetate, understqod that the mventmn res rm but are likewise applicable for coloring organic the Speclfic 3Z0 compound or cguphng component derivatives of cellulose in general, including the disclosed. For example, a y of the am m- T l hydrolyzed as well as the unhydrolyzed organic pounds of the invention previously described which contain a nuclear 'nitro group substituent may be reduced to the corresponding amino, applied to the fiber, diazotizcd: anddeveloped. in situacid esters such ascellulose formate, cellulose propionate, cellulose butyrate, cellulose acetatebutyrate, cellulose acetate-propionate and cellulose, and benzyl cellulose.
We claim:
1. The non-sulionated nuclear azo compounds having the general formula:
R1-N=NR2 wherein R1 represents an aryl nucleus of the benzene series, R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
wherein R represents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -R-OCONH2.
2. The non-sulfonated nuclear azo compounds having the general formula:
wherein R1 and R2 each represents an aryl nucleus of the benzene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
wherein R represents an aliphatic group joined to the molecule through a member selected from the group consisting of 1/ O J O 1 n n o-, N, fiN-, ON
and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -RO-CO-NH2. 3. The non-sulfonated nuclear azo compounds having the general formula:
wherein R1 represents an aryl nucleus of the benzene series, R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the formula:
wherein R represents an aliphatic group joined to the molecule through an oxygen atom.
4. The non-sulfonated nuclear azo compounds having the general formula:
wherein R1 and R2 each represents an aryl nucleus of the benzene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the formula:
wherein R represents an aliphatic group, R1 and R2 each represents a benzene nucleus, and R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group R-OCONH2.
6. The non-sulfonated nuclear azo compounds having the general formula:
:c R NOz-Ol =NR;1-N
I 11-0-0 O-NH: wherein each :1: represents a member selected from the group consisting of hydrogen, a halogen, a hydroxyl group, an alkyl group, and a nitro group, R represents an aliphatic group, R2 represents a benzene nucleus, and R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -RO-CONH2.
'7. Material made of or containing an organic derivative of cellulose colored with a dye selected from the group of non-sulfonated nuclear azo compounds having the general formula:
wherein R1 represents an aryl nucleus of the benzene series, R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
wherein R represents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group R- OCONH2.
8. Material made of or containing cellulose acetate colored with a dye selected from the group of non-sulfonated nuclear azo compounds having the general formula:
wherein R1 represents an aryl nucleus of the benzene series, R2 represents a member selected from the group consisting of an aryl nucleus of the benzene series, and an aryl nucleus of the naphthalene series, the said compounds containing in their molecule at least one amino group in position para to the azo group, and at least one group of the general formula:
wherein R rep-resents an aliphatic group joined to the molecule through a member selected from the group consisting of and a carbon atom of R, and wherein y represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -R-OCO-NH2.
9. Material made of or containing an organic derivative of cellulose colored with a dye selected from the class of non-sulfonated nuclear azo compounds having the general formula:
/Ra RiN=NR2N a-o-o O-NH:
wherein R represents an aliphatic group, R1 and R2 each represents a benzene nucleus, and R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group -RO-CONH2.
10. Material made of or containing cellulose acetate colored with a dye selected from the class of non-sulfonated nuclear azo compounds having the general formula:
iii
wherein R represents an aliphatic group, R1 and R2 each represents a benzene nucleus, and R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a hydroxyalkyl group, and the group --RO-CONH2.
11. Material made of or containing an organic derivative of cellulose colored with a dye selected from the class of non-sulfonated nuclear azo compounds having the general formula:
wherein m represents a member selected from the group consisting of hydrogen, a halogen, a hydroxyl group, an alkyl group, and a mtro group, R represents an aliphatic group, R2 represents a benzene nucleus, and R3 represents a member selected from the group consisting of hydrogen, an alkyl group, a. hydroxyalkyl group, and the group R-O--CONH2.
JOSEPH B. DICKEY. JOHN R. BYERS, JR.
US304138A 1939-11-13 1939-11-13 Azo compounds and material colored therewith Expired - Lifetime US2238486A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US304138A US2238486A (en) 1939-11-13 1939-11-13 Azo compounds and material colored therewith

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US304138A US2238486A (en) 1939-11-13 1939-11-13 Azo compounds and material colored therewith

Publications (1)

Publication Number Publication Date
US2238486A true US2238486A (en) 1941-04-15

Family

ID=23175220

Family Applications (1)

Application Number Title Priority Date Filing Date
US304138A Expired - Lifetime US2238486A (en) 1939-11-13 1939-11-13 Azo compounds and material colored therewith

Country Status (1)

Country Link
US (1) US2238486A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2424493A (en) * 1943-09-02 1947-07-22 Chem Ind Basel Pyrazolone monoazo dyes containing polybasic acid esters of alkylene sulfones
US2909561A (en) * 1956-07-18 1959-10-20 Sandoz Ag N-substituted urea and carbamate derivatives of water-insoluble tertiary amines
US3069408A (en) * 1956-07-18 1962-12-18 Sandoz Ltd Water-insoluble azo dyestuffs
US3869442A (en) * 1971-10-29 1975-03-04 Eastman Kodak Co Phenyl-azo-n-acylamidoethylaniline compounds
US3980636A (en) * 1971-10-29 1976-09-14 Eastman Kodak Company Phenyl-azo-aniline dyes
US4049378A (en) * 1974-02-18 1977-09-20 Bayer Aktiengesellschaft Dyestuff preparations
US4083685A (en) * 1973-06-02 1978-04-11 Bayer Aktiengesellschaft Process for dyeing synthetic fibre materials from an organic water-immiscible solvent
FR2405277A1 (en) * 1977-10-06 1979-05-04 Acna NEW WATER INSOLUBLE AZO COLORANTS

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2424493A (en) * 1943-09-02 1947-07-22 Chem Ind Basel Pyrazolone monoazo dyes containing polybasic acid esters of alkylene sulfones
US2909561A (en) * 1956-07-18 1959-10-20 Sandoz Ag N-substituted urea and carbamate derivatives of water-insoluble tertiary amines
US3069408A (en) * 1956-07-18 1962-12-18 Sandoz Ltd Water-insoluble azo dyestuffs
US3869442A (en) * 1971-10-29 1975-03-04 Eastman Kodak Co Phenyl-azo-n-acylamidoethylaniline compounds
US3980636A (en) * 1971-10-29 1976-09-14 Eastman Kodak Company Phenyl-azo-aniline dyes
US4083685A (en) * 1973-06-02 1978-04-11 Bayer Aktiengesellschaft Process for dyeing synthetic fibre materials from an organic water-immiscible solvent
US4049378A (en) * 1974-02-18 1977-09-20 Bayer Aktiengesellschaft Dyestuff preparations
FR2405277A1 (en) * 1977-10-06 1979-05-04 Acna NEW WATER INSOLUBLE AZO COLORANTS

Similar Documents

Publication Publication Date Title
US2373700A (en) Azo compounds and material colored therewith
US3487066A (en) Water-insoluble monoazo pyridine dyestuffs
US2821526A (en) Monoazo dyes
US2238486A (en) Azo compounds and material colored therewith
US2346013A (en) Azo compounds and material colored therewith
US2151857A (en) Water insoluble azo dyestuff
US2258977A (en) Azo compounds and material colored therewith
US2238485A (en) Azo compound and material colored therewith
US2261175A (en) Azo compounds and material colored therewith
US2206885A (en) Azo compounds and process for coloring therewith
US3405118A (en) 4-methoxy-6-nitrobenzothiazolylazo disperse dyes
US3586663A (en) Ethoxy ethyl amino phenyl azo dyestuff
US2234724A (en) Azo compounds and material colored therewith
US1975160A (en) Azo dyes and method for their preparation
US2211339A (en) Azo compounds and material colored therewith
US2391886A (en) Monoazo tetrahydroquinoline compounds
US2336275A (en) Azo dye compound
US2140538A (en) Coloration of organic derivatives of cellulose
US2200005A (en) Azo dye compounds and material colored therewith
US2231021A (en) Azo compounds and material colored therewith
US3398136A (en) Benzophenone monoazo dyes
US2140537A (en) Azo compounds and process for coloring therewith
US2227977A (en) Azo compounds and material colored therewith
US2249774A (en) Azo compound and material colored therewith
US2554443A (en) Azo safranine leather dyestuffs